Data / Medical devices / China / Daichuan Medical (Shenzhen) Co., Ltd
Daichuan Medical (Shenzhen) Co., Ltd: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance
Daichuan Medical (Shenzhen) Co., Ltd is registered with the FDA (registration 3018258446) in Shenzhen Guangdong, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 2, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3018258446
- Address
- Section 401A2, 506, Building 1, Shenzhen Biomedical Innovation Industrial Park, No. 14, Jinhui Road, Kengzi street, Pingshan District,Shenzhen, China., Shenzhen Guangdong, China, 518100
- Owner or operator
- Daichuan Medical (Shenzhen) Co., Ltd (10081773)
- Roles
- Manufacturer
- First device listed
- May 14, 2021
- Registered through
- 2026
- Brand names listed
- Camera System, XZING-S2, Disposable Colonoscope, XZING-C200B, Disposable GI Endoscope, XZING-W200B
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Colonoscope And Accessories, Flexible/Rigid | FDF | 2 | Manufacturer | accessdata.fda.gov |
| Gastroscope And Accessories, Flexible/Rigid | FDS | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| September 2, 2020 | K192704 | Endofresh Digestive Endoscopy System | FDS | Substantially Equivalent | Huizhou Xzing Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Gastroscope And Accessories, Flexible/Rigid
- All makers of Colonoscope And Accessories, Flexible/Rigid
Updated September 2, 2020. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.